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FAM58A gene
Known as:
FAM58A
, MGC29729
, FLJ21610
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National Institutes of Health
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Related topics
Related topics
1 relation
GAREM1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail
Caiye Zhu
,
Ming-na Li
,
S. Qin
,
F. Zhao
,
Suli Fang
Asian-Australasian journal of animal sciences
2019
Corpus ID: 198244907
Objective Chinese indigenous sheep breeds can be classified into the following three categories by their tail morphology: fat…
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Review
2017
Review
2017
The awakening of the CDK10/Cyclin M protein kinase
Vincent J Guen
,
C. Gamble
,
J. Lees
,
P. Colas
Oncotarget
2017
Corpus ID: 1975956
Cyclin-dependent kinases (CDKs) play important roles in the control of fundamental cellular processes. Some of the most…
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2017
2017
Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype
N. Boczek
,
T. Kruisselbrink
,
+4 authors
B. Lanpher
American journal of medical genetics. Part A
2017
Corpus ID: 19506350
STAR syndrome is a rare X‐linked dominant disorder characterized by toe Syndactyly, Telecanthus, Anogenital malformations, and…
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2016
2016
STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis
Vincent J Guen
,
C. Gamble
,
+5 authors
P. Colas
Cell cycle
2016
Corpus ID: 25765711
ABSTRACT CDK10/CycM is a protein kinase deficient in STAR (toe Syndactyly, Telecanthus and Anogenital and Renal malformations…
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2008
2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
S. Unger
,
D. Böhm
,
+18 authors
J. Kohlhase
Nature Genetics
2008
Corpus ID: 205357816
We identified four girls with a consistent constellation of facial dysmorphism and malformations previously reported in a single…
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